Canonical Allele Identifier: CA398317360
Gene: NOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1315431605
gnomAD v2: 17-26131336-C-A
MyVariant Identifiers: chr17:g.26131336C>A (hg19) chr17:g.27804310C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804310C>A , CM000679.2:g.27804310C>A GRCh38
NC_000017.10:g.26131336C>A , CM000679.1:g.26131336C>A GRCh37
NC_000017.9:g.23155463C>A NCBI36
NG_011470.1:g.1220G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.251G>T ENSP00000462879.1:p.Gly84Val
XM_011524859.1:c.-261G>T XP_011523161.1:n.-261G>T
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